Evidence map›Paper›PMID 32404512›Full record

ArticlemSphere2020

Can Unconventional Immunomodulatory Agents Help Alleviate COVID-19 Symptoms and Severity?

Stephen W Mamber, Steven Krakowka, Jeffrey Osborn, Lloyd Saberski, Ryan G Rhodes, Albert E Dahlberg, Sunthorn Pond-Tor, Kara Fitzgerald, Neal Wright, Sarah Beseme and 1 more

Open access · goldAbstract read
In one paragraph

Article in mSphere, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.6field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 23 citations in OpenAlex.

  1. Substances of abuse and their effect on SAR-CoV-2 pathogenesis.NeuroImmune pharmacology and therapeutics · 2023
    Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. The effect of estrogen in coronavirus disease 2019.American journal of physiology. Lung cellular and molecular physiology · 2021
    Review
  8. Article
  9. Review
  10. International journal of molecular sciences · 2021
    Review
  11. Article
  12. Article
  13. Drug target insights
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 7 institutions in 1 country.

Stephen W MamberThe Institute for Therapeutic Discovery, Delanson, New York, USA.
Steven KrakowkaThe Ohio State University, Columbus, Ohio, USA.
Jeffrey OsbornThe University of Kentucky, Lexington, Kentucky, USA.
Lloyd SaberskiYale University, New Haven, Connecticut, USA.
Ryan G RhodesThe University of North Carolina-Wilmington, Wilmington, North Carolina, USA.
Albert E DahlbergBrown University, Providence, Rhode Island, USA.
Sunthorn Pond-TorBrown University, Providence, Rhode Island, USA.
Kara FitzgeraldSandy Hook Clinic, Sandy Hook, Connecticut, USA.
Neal WrightCMC Biosciences, Beverly, Massachusetts, USA.
Sarah BesemeBeech Tree Labs, Providence, Rhode Island, USA.
John McMichaelThe Institute for Therapeutic Discovery, Delanson, New York, USA jm@beechtreelabs.com.
Brown University · USThe Institute for Therapeutic Discovery · USProvidence College · USThe Ohio State University · USUniversity of Kentucky · USUniversity of North Carolina Wilmington · USYale University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS coronavirus 2, or SARS-CoV-2) is the cause of the respiratory infection known as COVID-19. From an immunopathological standpoint, coronaviruses such as SARS-CoV-2 induce increased levels of a variety of T-helper 1 (Th1) and inflammatory cytokines and chemokines, including interleukin-1 (IL-1), IL-6, CCL2 protein, and CXCL10 protein. In the absence of proven antiviral agents or an effective vaccine, substances with immunomodulatory activity may be able to inhibit inflammatory and Th1 cytokines and/or yield an anti-inflammatory and/or Th2 immune response to counteract COVID-19 symptoms and severity. This report briefly describes the following four unconventional but commercially accessible immunomodulatory agents that can be employed in clinical trials to evaluate their effectiveness at alleviating disease symptoms and severity: low-dose oral interferon alpha, microdose DNA, low-dose thimerosal, and phytocannabinoids.

Indexed as

ImmunomodulationBetacoronavirusCannabinoidsCoronavirus InfectionsCOVID-19COVID-19 Drug TreatmentCytokinesDNAHumansInterferon-alphaPandemicsPhytochemicalsPneumonia, ViralSARS-CoV-2ThimerosalCannabinoidsCytokinesDNAInterferon-alphaPhytochemicalsThimerosalCOVID-19immunomodulatory agentsinterferon alphaphytocannabinoidsSARS-CoV-2thimerosal

Identifiers

PMID32404512
PMCPMC7227768
OpenAlexW3014506948

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.